Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic Epoxides
In a one-step procedure, various β-bromoalcohols were synthesized from natural terpenes in good to excellent yields. Using different catalysts, the reaction was carried out at room temperature, with H2O as nucleophile and N-bromosuccinimide as a bromine source under mild reaction conditions. The syn...
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doaj-9fbd98611faf4fa0a3a858bc263c46e12020-11-25T02:44:56ZengHindawi LimitedJournal of Chemistry2090-90632090-90712019-01-01201910.1155/2019/92685679268567Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic EpoxidesSaadia Oubaassine0Angela Köckritz1Reinhard Eckelt2Andreas Martin3Mustapha Ait Ali4Larbi El Firdoussi5Leibniz-Institut für Katalyse e. V. (LIKAT Rostock), Albert-Einstein-Str. 29 a, 18059 Rostock, GermanyLeibniz-Institut für Katalyse e. V. (LIKAT Rostock), Albert-Einstein-Str. 29 a, 18059 Rostock, GermanyLeibniz-Institut für Katalyse e. V. (LIKAT Rostock), Albert-Einstein-Str. 29 a, 18059 Rostock, GermanyLeibniz-Institut für Katalyse e. V. (LIKAT Rostock), Albert-Einstein-Str. 29 a, 18059 Rostock, GermanyDepartment of Chemistry, Equipe de Chimie de Coordination et Catalyse, Faculty of Sciences Semlalia, Cadi Ayyad University, P.O. Box: 2390, 40001 Marrakech, MoroccoDepartment of Chemistry, Equipe de Chimie de Coordination et Catalyse, Faculty of Sciences Semlalia, Cadi Ayyad University, P.O. Box: 2390, 40001 Marrakech, MoroccoIn a one-step procedure, various β-bromoalcohols were synthesized from natural terpenes in good to excellent yields. Using different catalysts, the reaction was carried out at room temperature, with H2O as nucleophile and N-bromosuccinimide as a bromine source under mild reaction conditions. The synthesized β-bromoalcohols were subsequently converted in situ to the corresponding epoxides in good yields.http://dx.doi.org/10.1155/2019/9268567 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Saadia Oubaassine Angela Köckritz Reinhard Eckelt Andreas Martin Mustapha Ait Ali Larbi El Firdoussi |
spellingShingle |
Saadia Oubaassine Angela Köckritz Reinhard Eckelt Andreas Martin Mustapha Ait Ali Larbi El Firdoussi Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic Epoxides Journal of Chemistry |
author_facet |
Saadia Oubaassine Angela Köckritz Reinhard Eckelt Andreas Martin Mustapha Ait Ali Larbi El Firdoussi |
author_sort |
Saadia Oubaassine |
title |
Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic Epoxides |
title_short |
Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic Epoxides |
title_full |
Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic Epoxides |
title_fullStr |
Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic Epoxides |
title_full_unstemmed |
Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic Epoxides |
title_sort |
catalytic β-bromohydroxylation of natural terpenes: useful intermediates for the synthesis of terpenic epoxides |
publisher |
Hindawi Limited |
series |
Journal of Chemistry |
issn |
2090-9063 2090-9071 |
publishDate |
2019-01-01 |
description |
In a one-step procedure, various β-bromoalcohols were synthesized from natural terpenes in good to excellent yields. Using different catalysts, the reaction was carried out at room temperature, with H2O as nucleophile and N-bromosuccinimide as a bromine source under mild reaction conditions. The synthesized β-bromoalcohols were subsequently converted in situ to the corresponding epoxides in good yields. |
url |
http://dx.doi.org/10.1155/2019/9268567 |
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